Reelin Rescues Behavioral, Electrophysiological, and Molecular Metrics of a Chronic Stress Phenotype in a Similar Manner to Ketamine

Abstract Over the past decade, ketamine, an NMDA receptor antagonist, has demonstrated fast-acting antidepressant effects previously unseen with monoaminergic-based therapeutics. Concerns regarding psychotomimetic effects limit the use of ketamine for certain patient populations. Reelin, an extracellular matrix glycoprotein, has shown promise as a putative fast-acting antidepressant in a model of chronic stress. However, research has not yet demonstrated the changes that occur rapidly after peripheral reelin administration. To address this key gap in knowledge, male Long–Evans rats underwent a chronic corticosterone (CORT; or vehicle) paradigm (40 mg/kg, 21 d). On day 21, rats were then administered an acute dose of ketamine (10 mg/kg, i.p.), reelin (3 µg, i.v.), or vehicle. Twenty-four hours after administration, rats underwent behavioral or in vivo electrophysiological testing before killing. Immunohistochemistry was used to confirm changes in hippocampal reelin immunoreactivity. Lastly, the hippocampus was microdissected from fresh tissue to ascertain whole cell and synaptic-specific changes in protein expression through Western blotting. Chronic corticosterone induced a chronic stress phenotype in the forced swim test and sucrose preference test (SPT). Both reelin and ketamine rescued immobility and swimming, however reelin alone rescued latency to immobility. In vivo electrophysiology revealed decreases in hippocampal long-term potentiation (LTP) after chronic stress which was increased significantly by both ketamine and reelin. Reelin immunoreactivity in the dentate gyrus paralleled the behavioral and electrophysiological findings, but no significant changes were observed in synaptic-level protein expression. This exploratory research supports the putative rapid-acting antidepressant effects of an acute dose of reelin across behavioral, electrophysiological, and molecular measures.


Introduction
Major depressive disorder (MDD) is the most prevalent neuropsychiatric disorder worldwide, affecting around 16% of people throughout their lifetime (Friedrich, 2017). Traditional monoaminergic-based antidepressants, such as selective serotonin reuptake inhibitors (SSRIs), have failed to fully address MDD, with around 50-60% of patients failing to respond to first-line treatment (Rush et al., 2006).
Ketamine, an NMDA receptor (NMDAR) antagonist, has rapid-acting antidepressant effects previously unseen (Berman et al., 2000;Zarate et al., 2006;Murrough et al., 2013;Dai et al., 2022). While there is significant debate on the exact mechanism of ketamine's antidepressant actions, they are generally thought to be mediated through an increase in cortical and hippocampal excitatory transmission (Abdallah et al., 2018;Duman et al., 2019;Gilbert and Zarate, 2020). Despite ketamine's success, there are still concerns regarding long-term use which may limit its widespread application to certain patient populations (Short et al., 2018;Alnefeesi et al., 2022).
The hippocampus is extremely susceptible to stress-induced impairments because of a high prevalence of glucocorticoid receptors in limbic regions (Herman et al., 2005). One of the main deficits observed is a decrease in hippocampal long-term potentiation (LTP), associated with a loss of learning and memory that is often observed in depression and depressive-like phenotypes (Kizilbash et al., 2002;Lynch, 2004). Ketamine has been shown to increase hippocampal LTP, learning, and memory in a fast-acting manner (Gilbert and Zarate, 2020;Sumner et al., 2020a,b). Reelin application has been able to rescue cognition, synaptic plasticity, and dendritic spinogenesis (Rogers et al., 2011(Rogers et al., , 2013Hethorn et al., 2015), but no research to our knowledge has assessed the effect of peripheral reelin administration on LTP after chronic stress.
In a chronic stress model, the decrease of reelin expression parallels the progressive development of depressivelike behavior (Lussier et al., 2013;Lebedeva et al., 2020;Sánchez-Lafuente et al., 2022). Previous research from our laboratory has demonstrated that reelin and ketamine have parallel effects on synaptoneurosomes (SNPs; isolated presynaptic and postsynaptic compartments) after in vitro treatment, dose-dependently increasing expression of PSD-95, mTORC1, and p-mTORC1 (Brymer et al., 2020;Johnston et al., 2020). However, no research has demonstrated changes after in vivo administration of reelin.
Administration of both traditional (chronic imipramine administration) and nontraditional (etanercept, a TNF-a inhibitor) antidepressants can rescue hippocampal reelin expression Brymer et al., 2018). Previous research from our laboratory has demonstrated that both repeated and acute intrahippocampal infusions of recombinant reelin (1 mg) were able to rescue stress-induced deficits in object-location memory, forced-swim test immobility, and hippocampal AMPAR, NMDAR, and GABA A R expression in the hippocampus. (Brymer et al., 2020). In addition, peripheral administration of reelin through the lateral tail vein demonstrated a parallel rescue of behavioral and biological chronic stress phenotype . The actions of reelin in chronic stress models may be activated through similar AMPAR-mediated downstream cellular signaling pathways to ketamine, as blocking AMPAR signaling with CNQX prevents reelin's ability to rescue a chronic stress phenotype (Brymer et al., 2020). Additionally, blockade of reelin's receptor apolipoprotein E receptor 2 and related downstream Src family signaling kinases prevented ketamine's actions in a depressive-like phenotype (Kim et al., 2021).
The aim of the present study is to provide an exploratory look at the behavioral, electrophysiological, and molecular effects of reelin in parallel to ketamine, to support reelin's putative actions in rescuing a chronic stress phenotype within 24 h.

Animal husbandry
Male Long-Evans rats (n ¼ 72) were purchased from Charles River Laboratories aged six weeks weighing between 200 and 250 g. Rats were housed individually with access to food and water ad libitum in clear polypropylene cages with a wooden chew cube and red hut. The colony was temperature-controlled at 21°C and maintained on a 12/12 h light/dark cycle that turned lights on at 7 A.M. Purina rat chow was maintained daily, and bedding was changed once per week.

Experimental procedures
All procedures were conducted in accordance with the Canadian Council on Animal Care and approved by the University of Victoria Animal Ethics Board. Rats were given one week of habituation to the facility before one week of daily handling. After weight was measured, animals were divided into 21 d of daily vehicle (NaCl, 0.9%, 2% polysorbate-80) or CORT (40 mg/kg suspended in vehicle, Steraloids). Rats were weighed daily to accurately administer injections at 1 ml/kg between 8 and 11 A.M.
On day 21, rats were administered an acute dose of vehicle (0.1 v PBS; pH 7.4), recombinant reelin (3 mg, intravenously, suspended in 0.5 ml vehicle), or ketamine hydrochloride (10 mg/kg, i.p., injected at 1 ml/kg in vehicle). The recombinant reelin (3820-MR-025-CF, R&D Systems) used is composed of reelin repeats 3-6 and dosed based on previous research from our lab showing that 3 mg is the most effective dose to rescue depressive-like behavior . An overview of all experimental procedures can be found in Figure 1.

Forced swim test
Animals who did not undergo in vivo electrophysiology (n ¼ 48) were administered a modified 1-d protocol of the forced swim test (FST), which has been previously described . A 1-d protocol controls for potential memory-based confounders that may be present in a more traditional 2-d protocol (Porsolt et al., 1978). Rats were placed in a Plexiglas swim tank (25 cm wide Â 25 cm long Â 60 cm high, filled to 30 cm) for 10 min. Water temperature was held at 27 6 2°C. Time spent swimming, climbing, immobile, and latency to immobility were all quantified through manual scoring.

Sucrose preference test
All animals (n ¼ 72) underwent the sucrose preference test (SPT), which is a commonly used indicator of anhedonia in animal models. On day 19, rats were habituated to two bottles of water accessible from their cage. Subsequently, they were habituated to two bottles of a sucrose solution (1%) to assess baseline drinking patterns. On the day of the test (day 21), rats were given free access to one bottle of water and one bottle of the sucrose solution for 24 h. Bottles were switched at 12 h to account for any location preferences, and weighed before and after the test.

Tissue preparation Perfusions
After behavioral tests on day 22, 24 of the animals were deeply anesthetized with isoflurane (5%) and transcardially perfused using 4% (w/v) paraformaldehyde (PFA) dissolved in 0.1v PB (pH 7.4). Brains were stored in the same PFA solution for 48 h at 4°C before being transferred to a 30% sucrose solution with 0.1% sodium azide. Brains were kept in the sucrose solution for at least 72 h before being sectioned in the coronal plane at 30 mm on a cryostat (CM1850 UV, Leica Biosystems) at À20°C. Coronal sections were stored in a cryoprotectant [30% (w/v) sucrose, 1% (w/v) polyvinylpyrrolidone, and 30% (v/v) ethylene glycol in 0.1 M PBS (pH 7.4)] at À20°C until immunohistochemical analyses. for 21 d (subcutaneously). On the 21st day, they were administered an injection of reelin (3 mg, i.v.), ketamine (10 mg/kg, i.p.), or vehicle (PBS). Twenty-four hours later, they underwent behavioral testing and killing for fresh or fixed tissue. The animals who underwent in vivo electrophysiology underwent a u burst stimulation protocol to induce LTP, which was recorded from the dentate gyrus. s.c., subcutaneous; MPP, medial perforant path; DG, dentate gyrus.

In vivo electrophysiology
On day 22, rats (n ¼ 24) were weighed and anesthetized deeply with urethane (1.5 g/kg, i.p.). Supplemental doses (0.3 ml) were given as necessary until loss of consciousness as determined through withdrawal reflex and respiratory rate. After rats were unconscious, they were placed on a stereotaxic frame (Kopf Instruments) with body temperature kept steady at 37°C using a regulated homeothermic control unit (Harvard Instruments). Tear gel was first applied before surgical incisions, and then again as needed. An incision was made along the dorsal surface of the skull to expose bregma in accordance with sterile protocols. Two holes were drilled anterior to the bregma for grounding electrode placement (stainless steel, 0.011" coated). Holes were also drilled for the recording (stainless steel, 0.008" coated; 3.5 mm posterior and 2.4 mm lateral to bregma) and stimulating (stainless steel, 0.011 mm coated; 7.4 mm posterior and 3.4 mm lateral to bregma) electrodes.
Baseline recordings were measured using a 0.12-ms pulse at 0.0067 Hz. Input/output (I/O) function was used to determine baseline excitatory transmission. Stable baseline recordings were required for at least 30 min before a u burst stimulation (TBS) protocol was applied to induce LTP. The TBS consisted of 10 bursts of five pulses (0.25 ms in duration) at 400 Hz with a 200-ms interburst interval, which was repeated four times in 30-s intervals. After induction of LTP, baseline stimulation was continued for 1 h. The slope of the rising phase (10-90%) of field EPSPs (fEPSPs) were recorded. To assess post-tetanic potentiation (PTP), fEPSPs were taken immediately after TBS. LTP was assessed through fEPSP slope from 55 to 60 min after TBS. All data are presented as mean percent change from prestimulation baseline. Confirmation of electrode placement was conducted via Cresyl Violet staining.
Reelin-IR cells were imaged using a Zeiss Axioimager M.2 and counted using an unbiased optical fractionator method (Stereo Investigator, 2022.2.1, MBF Bioscience). The area of interest was traced at 2.5Â magnification, with stereological analyses undertaken at 20Â magnification. Equations for number estimates have been previously described Allen et al., 2022).

Experimental design and statistical analyses
As the purpose of these experiments was primarily exploratory, and four animals/group were used for each separate biological experiment (electrophysiology, immunohistochemistry, Western blotting). The total number of male Long-Evans rats used was 72, and behavior was conducted on all rats that did not undergo electrophysiological analyses (n ¼ 48). Power analyses were used based on previous behavioral, immunohistochemistry and Western blotting data conducted in our lab, as well as an initial pilot electrophysiological experiment. The groups were as follows to control for both chronic and acute treatments: Vehicle/ Vehicle, Vehicle/Ketamine, Vehicle/Reelin, CORT/Vehicle, CORT/Ketamine, CORT/Reelin. Analyses across all experiments aside from Western blotting, which was analyzed in a three-way ANOVA (tissue type Â treatment Â condition), were conducted using two-way ANOVAs to assess the effects and differences between condition (chronic vehicle or CORT administration) and treatment group (acute administration of vehicle, reelin, or ketamine). To ensure proper representation of relative protein expression in Western blot analyses, technical duplicates or triplicates were analyzed for every protein from each animal. All statistics were conducted on SPSS (v27, IBM). Tukey's post hoc test was used for further comparisons. All data are presented as mean 6 SEM. Statistical significance and effect sizes (h 2 ) are reported in Table 1. A summary of findings can be found in Tables 1 and 2.

Forced swim test
In the forced swim test, significant differences were found in measures of swimming (F (2,41) ¼ 6.384, , and latency to immobility (F (1,41) ¼ 7.670, p ¼ 0.0084, h 2 ¼ 0.23; Fig. 2A-D). Post hoc analyses revealed that the CORT/vehicle group spent significantly more time immobile (p ¼ 0.0003), an increase that was rescued by reelin ( p ¼ 0.0049) and ketamine ( p ¼ 0.0047; Fig. 2C). In parallel to this, swimming time was decreased in rats treated with CORT/vehicle ( p ¼ 0.0002), which was upregulated by reelin ( p ¼ 0.0028) and ketamine ( p ¼ 0.0034; Fig. 2B). Finally, those in the CORT/vehicle subgroup had significantly shorter latency to immobility times when compared with vehicle-treated animals, which were rescued by reelin ( p ¼ 0.0423), but not ketamine (Fig. 2D). No effects on climbing behavior were found ( Fig. 2A).

Sucrose preference test
Sucrose consumption was measured during the habituation phase (day 20, two bottles of sucrose) and test phase of the SPT (day 21, one bottle of water and one bottle of sucrose) to determine anhedonic-like behavior. During the habituation phase, no significant differences were found between groups (Fig. 3A). In the test phase, significant group differences were found (F (2,56) ¼ 5.984, p ¼ 0.0044, h 2 ¼ 0.28) in sucrose consumption. The CORT/vehicle and vehicle/ketamine subgroups drank significantly less sucrose than vehicle animals ( p ¼ 0.009 and p ¼ 0.002, respectively), suggesting greater anhedonic-like behavior. In vivo electrophysiology I/O curve Increasing pulse widths (0.04, 0.08, 0.12, 0.16, 0.2, and 0.24 mA) were measured before baseline measurements and after a stable signal was found to determine input/ output (I/O) function. No significant differences were found in fEPSP slopes between any experimental subgroups, suggesting baseline synaptic excitability was Figure 2. Forced swim test. A, No significant differences were found across groups in FST climbing. B, CORT administration significantly decreased swimming in the FST, which was rescued by both reelin and ketamine. C, CORT administration significantly increased immobility in the FST, which was rescued by both reelin and ketamine. D, Latency to immobility in the FST was decreased by CORT but was rescued only by reelin administration. All data presented as mean 6 SEM; *p , 0.05, **p , 0.01, ***p , 0.001. similar. In all animals, the fEPSP slope was significantly greater with increased stimulation (Fig. 4A).

PTP and LTP
After a stable baseline was collected for a minimum of 30 min, the TBS protocol was used. Following TBS, the baseline stimulation protocol was continued for 1 h, with PTP defined as 1 min after TBS and LTP as 55-60 min after TBS. Mean traces of vehicle/vehicle, CORT/vehicle, CORT/reelin, and CORT/ketamine are graphed (Fig. 4B). Analyses were conducted on all 6 groups through a twoway ANOVA followed by Tukey's post hoc tests whether the initial ANOVA was significant. Significant group differences were found for PTP (F (2,18) ¼ 7.179, p ¼ 0.0051, h 2 ¼ 0.47) and LTP (F (2,18) ¼ 3.924, p ¼ 0.0385, h 2 ¼ 0.32). The CORT/vehicle subgroup demonstrated significantly lower PTP than vehicles ( p ¼ 0.0008), although this was not significantly rescued by reelin or ketamine (Fig. 4C). Interestingly, PTP in vehicle animals was decreased by both reelin (0.0415) and ketamine (0.0064). LTP was significantly decreased after CORT treatment ( p ¼ 0.0045) but was rescued by both reelin ( p ¼ 0.0342) and ketamine ( p ¼ 0.0493; Fig. 4D).

Reelin immunoreactivity in the subgranular zone
Early research demonstrated that reelin and ketamine can increase reelin immunoreactivity in the subgranular zone of the hippocampus within a few days (Brymer et al., 2020;Johnston et al., 2020;Allen et al., 2022). However, no assessments have determined whether this effect is observed within 24 h and may be associated with the rapid-acting behavioral effects observed with each therapeutic. Significant condition and treatment differences were found in reelin immunoreactivity (F (2,18) ¼ 3.732, p ¼ 0.0441, h 2 ¼ 0.33). Chronic CORT treatment significantly decreased the expression of reelin in the subgranular zone of the hippocampus ( p ¼ 0.0129), which was upregulated within 24 h by peripheral administration of both reelin ( p ¼ 0.0421) and ketamine ( p ¼ 0.0443; Fig.  5A,B).

Western blot analyses
Western blotting analyses were conducted to evaluate condition and treatment differences in both whole homogenate (WH) and SNP tissue for GluN2b, PSD-95, Synapsin I, and p-ERK1/2, p-mTOR, mTOR, ratio of active mTOR, p-GluA1, GluA1, ratio of active GluA1, p-CREB, CREB, and ratio of active CREB. No significant effects of the condition or treatment were found for all proteins measured (Figs. 6, 7).

Discussion
This exploratory study is the first to demonstrate that an acute peripheral dose of reelin is able to rescue behavioral, electrophysiological, and molecular deficits caused by chronic stress in a rapid-acting manner. These changes were found to be similar to those induced by ketamine, the current gold standard rapid-acting antidepressant. The dose of reelin used (3 mg) was found to be the most effective in rescuing behavioral and biological deficits in the CORT model, as demonstrated by previous research from our laboratory .
Behaviorally, reelin and ketamine rescued the increase in immobility and decrease in swimming induced by CORT in the FST, a proxy of despair-like behavior (Porsolt et al., 1978). Multiple previous studies have supported this finding after either reelin and ketamine administration (Fitzgerald et al., 2019;Brymer et al., 2020;Allen et al., 2022) and the FST is often used as an indicator of antidepressant efficacy in animal models (Kitada et al., 1981). Interestingly, the latency to immobility was rescued solely by reelin, which suggests animals receiving reelin may have improved performance relative to those receiving ketamine. The CORT-treated rats displayed greater anhedonic-like behavior than controls, however this was not significantly rescued by ketamine or reelin in this model. However, the vehicle animals who received ketamine also had significantly decreased sucrose consumption, a finding which parallels clinical trials in healthy volunteers who display greater depressive behaviors after ketamine administration (  . Sucrose consumption after chronic stress, reelin, and ketamine treatment. A, No significant differences were found in sucrose consumption across groups during habituation. B, During the test phase, rats treated with chronic CORT had a significantly decrease consumption of sucrose. In addition, vehicle rats treated with ketamine had significantly decreased sucrose consumption. No significant effect of reelin or ketamine was found. Data expressed as mean 6 SEM; **p , 0.01. To our knowledge, this study was the first to demonstrate that reelin can rescue hippocampal LTP in a chronic stress model. As previously described, LTP is an essential process for learning and memory, which are known to be negatively affected in depression (Strömgren, 1977;Weingartner et al., 1981;Kizilbash et al., 2002). Context discrimination and fear learning in particular have been associated with medial perforant path activity (Ferbinteanu et al., 1999), both of which are impacted in patients with depression and in chronic stress models (Britton et al., 2011;Camp et al., 2012;Wurst et al., 2021). Cortical and hippocampal increases in excitatory transmission have also been implicated in the efficacy of ketamine as an antidepressant (Zanos et al., 2018b;Gilbert and Zarate, 2020), and the parallel actions of reelin in this study provide further support for its putative rapid-acting antidepressantlike actions. Interestingly, ketamine administration decreased PTP in the control group, a finding that parallels the clinical research which demonstrates the deleterious effects of ketamine in healthy controls (Derntl et al., 2019;Nugent et al., 2019), perhaps because of its dissociative side effects. Reelin also caused a slight decrease in PTP in controls, but this reduction was not at the same magnitude as ketamine. As reelin was administered peripherally, conclusions cannot be made about the direct electrophysiological actions of reelin in the hippocampus. However, because of the high weight of reelin, hippocampal tissue damage and low diffusion rates from direct administration could impact the quality of electrophysiological signals.
The molecular indicators of antidepressant-like efficacy demonstrated more mixed results. Chronic CORT administration decreased reelin immunoreactivity in the subgranular zone of the dentate gyrus, a finding paralleled by previous research (Lussier et al., 2011(Lussier et al., , 2013Lebedeva et al., 2020). The ability of either reelin or ketamine to rescue reelin expression has also been previously demonstrated Kim et al., 2021;Allen et al., 2022); however, these changes had not yet been noted within 24 h as shown in this study. Despite previous research showing changes in SNPs after Figure 4. In vivo electrophysiological recordings from vehicle, CORT, reelin, and ketamine administered rats. A, I/O function was measured using increasing pulse widths to determine baseline excitability. No differences were found between treatment groups. B, Average fEPSP slope as a % change from baseline for vehicle/vehicle, CORT/vehicle, CORT/reelin, and CORT/ketamine experimental groups. A stable baseline was recorded for 30 min. u Burst stimulation (TBS) was applied at 0 min. Post-tetanic potentiation (PTP) was measured at 1 min after u burst stimulation (TBS) and long-term potentiation (LTP) was measured 55-60 min after TBS. C, Changes in PTP potentiation after TBS. CORT significantly decreased PTP, which was not rescued by reelin or ketamine. D, Changes in LTP after TBS. CORT administration significantly decreased LTP, which was rescued by both reelin and ketamine. All data expressed as mean 6 SEM; *p , 0.05, **p , 0.01, ***p , 0.001. reelin and ketamine administration (Li et al., 2010;Johnston et al., 2020), no significant changes were measured in this context. Of note, the previous changes observed in SNPs after in vivo administration of ketamine disappeared by ;2 h postinjection (Li et al., 2010). Previous in vitro assessments of reelin found changes after 30 min , suggesting the time course of this research may have missed synaptic-specific changes in response to rapid-acting therapeutics.
There are still many questions regarding how a peripherally administered dose of reelin can have rapid-acting antidepressant effects and provoke changes in the CNS within 24 h after administration. Previous research has found evidence of reelin in the caveolae of endothelial cells and associated with the luminal side of the plasma membrane (Perez-Costas et al., 2015). This evidence suggests that despite its large size (410 kDa), reelin may cross the blood-brain barrier (BBB) through a receptormediated transcytosis mechanism. In addition, leakage of the BBB has been reliably found in depression, where increased permeability may allow for the crossing of molecules that are unable to in healthy controls (Najjar et al., 2013;Dudek et al., 2020). Reelin signaling through Dab1 activity has also been identified as a modulator of the BBB, organizing neuro-glia-vessel communication to support BBB integrity, and prevent leakage of interleukin-6 after chronic stress (Segarra et al., 2018;Zhang et al., 2020).
After crossing the BBB, tight gap junctions, pericytes, and astrocytic endfeet would most likely prevent the diffusion of reelin. However, evidence has shown that a unilateral intrahippocampal infusion of reelin is able to rapidly rescue deficits in both hemispheres, suggesting the activation of cellular signaling pathways can reverse deficits throughout the brain (Brymer et al., 2020). This could potentially be mediated through an increase in AMPAR throughput, as demonstrated by previous research which ascertained the administration of NBQX blocks therapeutic effects after an intrahippocampal infusion of reelin. While not observed here, increases in mTORC1 and ERK signaling have been observed after reelin administration in vitro, and warrant further investigation (Brymer et al., 2020;Johnston, J.N., Caruncho, H.J., and Kalynchuk, L.E., unpublished data). Future research should ascertain the exact mechanisms by which peripheral reelin is able to rescue behavioral and electrophysiological deficits through the blockade of AMPAR and NMDAR throughput, as well as mTORC1 and ERK signaling, which have all been associated with ketamine's rapid-acting antidepressant actions (Zanos and Gould, 2018).
In addition, the peripheral mechanisms by which reelin could influence central protein translation are yet unknown. Reelin is expressed in blood plasma through platelet secretion, which has been associated with hemostasis and inflammatory responses (Tseng et al., 2014). Reelin has also been demonstrated to alter the membrane protein clustering (MPC) of the serotonin transporter (SERT) both in vitro and in vivo Allen et al., 2022). SERT is a primary target of conventional antidepressants, and parallel changes in SERT MPC have been observed in the chronic CORT model and treatment-naive participants with depression (Romay-Tallon et al., 2018). Reelin may also have its rapid-antidepressant-like actions through crossing the BBB and/or a reduction in the inflammatory response.
This study aimed to present a broad exploration of the changes induced in behavioral, electrophysiological, and molecular measures 24 h after acute peripheral reelin administration. Ketamine was used as an active comparator, as it is the current gold standard in rapid-acting antidepressant treatment. Given the exploratory nature of this study, small sample sizes may have limited statistical power that prevented the observation of subtle differences. Additionally, while chronic CORT administration is a reliable and validated model for the study of depression (Gregus et al., 2005;Johnson et al., 2006;Gourley and Taylor, 2009;Marks et al., 2009;Sterner and Kalynchuk, 2010), animal models are unable to completely mimic every facet of clinical depression which limits translation (McKinney and Bunney, 1969;Tkacs and Thompson, 2006). Treatment-resistant depression, the most common indication for use of rapid-acting antidepressants, is particularly difficult to model (Willner and Belzung, 2015). . Reelin expression in the subgranular zone after reelin and ketamine administration. A, Unbiased stereology estimates of reelin cell population in the dentate gyrus subgranular zone. CORT administration significantly decreased reelin expression, which was rescued by an acute dose of reelin and ketamine. B, Representative photomicrographs of reelin expression in the subgranular zone. All data expressed as mean 6 SEM; *p , 0.05. Figure 6. The effect of CORT, reelin, and ketamine treatment on whole cell and synaptic proteins (part I). A, Whole cell p-mTOR expression was increased after ketamine administration. B-J, No significant differences were found between any treatment groups for all proteins and activity ratios measured. V, vehicle; R, reelin; K, ketamine; C, CORT; WH, whole homogenate; SNP, synaptoneurosomes. All data are expressed as mean 6 SEM; *p , 0.05.
Future research needs to expand on these preliminary findings and use a broad spectrum of animal models to assess reelin's putative rapid-acting effects. Attaining a homeostatic balance of reelin, which is known to be downregulated in depression and other neuropsychiatric disorders, is imperative. While this study administered a low dose of reelin to upregulate reelin signaling and ameliorate behavior associated with chronic stress, significant Figure 7. The effect of CORT, reelin, and ketamine treatment on whole cell and synaptic proteins (part II). A-E, No significant differences were found between any treatment groups for all proteins measured. V, vehicle; R, reelin; K, ketamine; C, CORT; WH, whole homogenate; SNP, synaptoneurosomes. All data are expressed as mean 6 SEM; *p , 0.05. increases in reelin expression can be a risk factor for the development of certain cancers and hepatic fibrosis (Khialeeva and Carpenter, 2017). In addition, determining the time scale of reelin's effects is essential, as ketamine is known to act within 1 h and up to two weeks after administration (Murrough et al., 2013;Kishimoto et al., 2016). To our knowledge, no research has ascertained the length of reelin's effects in a chronic stress model. In conclusion, this work provides multiple perspectives on how reelin may act as a putative rapid-acting treatment for chronic stress in a similar manner to ketamine, the gold standard for clinical antidepressant treatment.